Use of Electronic Informed Consent in Clinical Investigations β Questions and Answers: Guidance for Institutional Review Boards, Investigators, and Sponsors From Food and Drug Administration (FDA) πΊπΈ This document is a guidance document titled "Use of Electronic Informed Consent in Clinical Investigations β Questions and Answers". It falls under the topic of "Administrative / Procedural". Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage filled Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on January 26, 2021 Other (Public Domain) 0 reuses 0 favorites